Binding of amyloid β precursor protein to coagulation factor XIa in vivo may favour haemorrhagic stroke

被引:4
作者
Bornebroek, M
von dem Borne, PAK
Haan, J
Meijers, JCM
Van Nostrand, WE
Roos, RAC
机构
[1] Leiden Univ, Med Ctr, Dept Neurol K5Q97, NL-2300 RC Leiden, Netherlands
[2] Univ Utrecht Hosp, Dept Haematol, Utrecht, Netherlands
[3] Rijnland Hosp, Dept Neurol, Leiderdorp, Netherlands
[4] SUNY Stony Brook, Ctr Hlth Sci, Dept Med & Pathol, Stony Brook, NY 11794 USA
关键词
hereditary cerebral haemorrhage with amyloidosis; Dutch type (HCHWA-D); beta precursor protein; factor XI; amyloid; cerebral haemorrhage;
D O I
10.1007/s004150050188
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D), caused by a mutation at codon 693 in the amyloid beta precursor protein (beta PP) gene, is clinically characterised by haemorrhagic strokes and dementia. The secreted forms beta PP751 and beta PP770 are identical to protease nexin II (PNII), which is a potent inhibitor of intrinsic blood coagulation factor XIa in vitro. We investigated the concentration of complexes between factor XIa and beta PP in vivo, to search for a possible cause of the haemorrhagic strokes in HCHWA-D. In this prospectively designed study, first an enzyme-linked immunosorbent assay (ELISA) was performed with dilutions of the factor XIa-beta PP complexes prepared from platelets as a standard curve. By means of this ELISA, the concentration of factor XIa-beta PP complexes was measured in plasma samples. Second, plasma of 23 HCHWA-D patients and 23 healthy controls was collected, and the concentration of complexes was measured with this method. The mean concentration of factor XIa-beta PP complexes in plasma of HCHWA-D patients (mean 13.73 U/ml; SD 4.78) was significantly (P = 0.05) higher than the concentration in plasma of healthy controls (mean 11.37; SD 2.77). The differences, however, were small and there was a major overlap between the concentrations in patients and controls. In HCHWA-D mutation carriers, the concentration of factor XIa-beta PP complexes was not related to age, and there was no difference between presymptomatic and symptomatic mutation carriers. From this study, it can be concluded that beta PP forms complexes with factor XIa in vivo both in HCHWA-D patients and in normal controls. The concentration in HCHWA-D patients was higher. This is probably the result of diffusion of complexes from the cerebral circulation into plasma. Elevated beta PP in cerebrovascular amyloid deposits is possibly a local factor contributing to the development of haemorrhagic strokes.
引用
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页码:111 / 115
页数:5
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